THE BREEDING OF A PARADISE FLYCATCHER

1. At Amani, Tanganyika Territory, the Paradise Flycatchers use the softest moss for their nests and make them durable by oversewing the rim with cobweb. Sites are on the forest edge nearly always over water. Theree hours of observation were made at three nests in spells of about eight hours at a time.
2. On the whole the males and females shared the care of the eggs and the young about equally, but there were wide differences in this respect from day to day
3. The eggs were covered for over 90% of the observed time, and a high proportion of spells "on" were terminated by thc mate's arriving to take over. Duration of individual spells "on" varied up to two hours, but the favourite duration (nearly half of all the spells) was about 30–40 minutes. This applied both to spells "on" terminated by the initiative of the sitting bird and to those terminated by the arrival of the mate. The possibility suggests itself that an internal rhythm was operating, irrespective of whether a bird was on or off the nest. Nevertheless, out of 39 occasions (all short) when the eggs were uncovered through the sitter's departure without relief, the same bird returned on 18, which suggests that when off the nest both parents "keep an eye on it" and react to the situation "nest uncovered".
4. Brooding of the young amounted at first to nearly the same high percentage of time as the brooding o f the rggs, but was in much shorter spells. It stopped abruptly about the fifth day. others followed a parent.
5. Each nestling of a brood of two in a nest received more food (largely butterflies) than each in two broods of three, 2.6-5.4 feeds per hour compared with 14-2.5 and 1.3-1.8.
6. Some of the young that wcre seen to fly left the nest in the absence of the parents, All left between dawn and noon. Nestling period about 11 days irrespective of the amount of food received.     

4. UNUSUAL EXPERIENCES WITH BIRDS

Earlé, R. A. 1989. Breeding biology of the Redbreasted Swallow Hirundo semirufa. Ostrich 60: 13–21.

The two races of the Redbreasted Swallow Hirundo semirufa seem to have separate breeding seasons with the northern race H. s. gordoni breeding April-July, while most records for the nominate race fall in October-February. All nests studied were in concrete culverts less than 1 m high. Eggs laid in second clutches by individual females weighed significantly less than eggs laid in first clutches. Eggs hatched on average 16,2 days after incubation started or 18–21 days after the eggs were laid. Only females incubated. Chicks fledged 23–25 days after hatching and reached a maximum body mass of about 31,5 g on day 18 before a steady decline in mass until fledging. Most nesting failures resulted from infertile eggs or starvation of young in the nest (16,2% of all young starved). Overall breeding success was 60,6%. In all, 81,8% of first clutches produced fledglings but only 44,4% of second clutches. Over a three year period 4,9 young were produced per pair breeding in the area (1,6 young/pair/breeding season).     

The social system of the Pale Chanting Goshawk Melierax canorus; monogamy v polyandry and delayed dispersal

The social organization and reproductive strategy of the Pale Chanting Goshawk Melierax canorus were investigated in four southern African study areas. Territories supporting adults additional to the breeding pair were observed in two study areas. Within one of these areas, these additional adults were either non-breeders staying in their natal territory but actively excluded from the nesting area during the breeding season or a male cobreeder participating fully in reproductive activities with the breeding pair. Polyandrous trios were, however, observed in only one vegetation type in this area, Broken Veld. The annual number of offspring fledged per group did not differ significantly between vegetation types nor between polyandrous trios and monogamous pairs within Broken Veld. Pale Chanting Goshawks lay predominantly two-egg clutches. In 2 out of 5 years, breeding groups succeeded in laying, hatching and even fledging a second brood of young after successfully fledging their first brood. Double brooding occurred more frequently in Broken Veld and most frequently in polyandrous trios in this vegetation type. To accommodate their relatively long breeding cycle (>115 days) in this temperate study area with its limiting summer breeding period, double-brooding Pale Chanting Goshawks laid the first clutch in midwinter and the second, on average, 24 days after the offspring from the first brood left the nest.     

Reproductive tactics of the ringed plover Charadrius hiaticula

Reproductive tactics of ringed plovers Charadrius hiaticula were studied at three localities in SW Sweden during five seasons. The usual clutch size is four, but removal experiments showed that females can produce five eggs in succession, with similar intervals between all eggs. High predation made mean breeding success per clutch low, 6.3% of eggs resulting in fledged young. Replacement clutches were common, and many pairs laid again after rearing their first brood to fledging. Egg laying spanned three months, much longer than for other waders in this region. Between years, reproductive success varied unpredictably with time of the season, but averaged over several years, the expected success was low and similar for the different parts of the breeding season. Chicks from late clutches had similar survival and recruitment as others. Because of the long breeding season and high rate of nest failure a female may produce up to five clutches of four eggs per season, containing in total about 3.7 times her own mass. Yearly local survival of adult females and males was estimated to 84.6 and 88.6%, respectively. Ability to produce many clutches with similar expected success throughout the season favours a long reproductive period, sometimes leading to double-brooding. Possible life-history trade-offs are discussed.     

Females compensate for moult‐associated male nest desertion in Hooded Warblers

Uniparental offspring desertion occurs in a wide variety of avian taxa and usually reflects sexual conflict over parental care. In many species, desertion yields immediate reproductive benefits for deserters if they can re‐mate and breed again during the same nesting season; in such cases desertion may be selectively advantageous even if it significantly reduces the fitness of the current brood. However, in many other species, parents desert late‐season offspring when opportunities to re‐nest are absent. In these cases, any reproductive benefits of desertion are delayed, and desertion is unlikely to be advantageous unless the deserted parent can compensate for the loss of its partner and minimize costs to the current brood. We tested this parental compensation hypothesis in Hooded Warblers Setophaga citrina, a species in which males regularly desert late‐season nestlings and fledglings during moult. Females from deserted nests effectively doubled their provisioning efforts, and nestlings from deserted nests received just as much food, gained mass at the same rate, and were no more likely to die from either complete nest predation or brood reduction as young from biparental nests. The female provisioning response, however, was significantly related to nestling age; females undercompensated for male desertion when the nestlings were young, but overcompensated as nestlings approached fledging age, probably because of time constraints that brooding imposed on females with young nestlings. Overall, our results indicate that female Hooded Warblers completely compensate for male moult‐associated nest desertion, and that deserting males pay no reproductive cost for desertion, at least up to the point of fledging. Along with other studies, our findings support the general conclusion that late‐season offspring desertion is likely to evolve only when parental compensation by the deserted partner can minimize costs to the current brood.     

Nest, but Not Egg, Fidelity in a Territorial Salamander

Egg recognition and subsequent egg brooding are costly forms of parental investment in many species of vertebrates. Life history factors, such as coloniality or risk of brood parasitism, may constrain egg recognition in vertebrates. Female red-backed salamanders ( Plethodon cinereus ) from my study site are territorial and do not share nest sites with other females. They are terrestrial and neither they nor their eggs are likely to be displaced by environmental factors such as flooding. I experimentally tested, in the laboratory, the hypothesis that female red-backed salamanders can discriminate between their own eggs and the eggs of unfamiliar females. Each female was allowed to move about a test chamber containing two clutches of eggs, one clutch with which it was found in the forest and one that had been found with a distant female. Most females remained with one clutch of eggs, which they brooded during the entire observation period. However, they did not significantly prefer to brood their own eggs over the eggs of another female. In a corollary field experiment, I tested whether brooding females that were displaced 1 m from their nest sites would return to their territories and commence brooding behaviour within 3 d. All 10 displaced females returned to their own nest within this time period and were found brooding their eggs. Because female red-backed salamanders at my study site do not tend to share nest sites with other females and because their eggs remain in stationary nests, selection may not have favoured egg recognition. However, the results suggest that female salamanders indirectly recognize their own eggs by actively recognizing their territorial nest sites.     

An experimental analysis of joint nesting in the salamander Hemidaetylium scutatum (Caudata: Plethodontidae): the effects of population density

Three nesting behaviour patterns are documented in the plethodontid salamander Hemidactylium scutatum. A female may lay eggs (1) in a solitary nest and brood them, (2) in a joint nest and brood them as well as eggs of other females, or (3) in a joint nest that is brooded by another female. The hypothesis that population density was positively associated with joint nesting was tested by following two populations for 5 years and by experimentally manipulating the population density of nesting females in artificial habitats for the latter 2 years. The proportion of joint nests did not vary with density, although joint nests tended to contain eggs of more females at the high population density. Joint nests were usually brooded by one female; thus, most females that laid eggs in joint nests did not brood them at high density. The reproductive success, as measured by survival of embryos, of solitary and joint nesters was equivalent. Joint nests were deserted less often, however, which decreased the probability of catastrophic mortality. The number of days of brooding was significantly positively correlated with loss of body mass of females, suggesting a cost to brooding behaviour. Joint nesting with solitary brooding is not explained by aggressive usurpation of nests or by brood parasitism.     

THE BIRDS OF LANGEBAAN LAGOON

Data are presented on breeding success of Red Bishops (Euplectes orix) collected over four breeding seasons at a colony in the Addo Elephant National Park, Eastern Cape, South Africa. Overall hatching and fledging success were 53.8% and 26.0% of all eggs laid, respectively, and the overall mean number of fledglings per breeding attempt was 0.77. Hatching and fledging success varied significantly among seasons, with both clutch and brood losses due to predation being the main reason for the observed differences. Hatching success also differed significantly among clutch sizes, being highest for four-egg clutches (63.2%), intermediate for three-egg clutches (55.5%) and lowest for two-egg clutches and five-egg clutches (33.2% and 34.3%, respectively). However, fledging success was not significantly different among clutch sizes. The mean number of fledglings per breeding attempt was 0.44 for two-egg clutches, 0.80 for three-egg clutches, 1.10 for four-egg clutches, and 0.57 for five-egg clutches. The height of accepted nests (i.e.nests in which at least one egg was laid) was significantly lower than the height of nests not accepted. In addition, accepted nests in which eggs hatched and young fledged were significantly lower than accepted nests in which no eggs hatched and no young fledged. These overall effects of nest height on nest acceptance and hatching and fledging success were, however, due only to nests built above water, since no such effects were found when nests built above ground (i.e.on dry land) were analysed separately. I detected no effect of nest coverage on the probability of a nest being accepted, nor was there any effect of nest coverage on hatching or fledging success. Nests above water were significantly more likely to be accepted than nests above ground; however, hatching and fledging success of nests that were accepted did not differ significantly between nests built above water and those built above ground.     

Breeding behaviour and performance of the Knysna Warbler Bradypterus sylvaticus on the Cape Peninsula,South Africa

Three pairs of Knysna Warblers were monitored on the south-eastern slopes of Table Mountain during the 2000 breeding season. Males displayed alone on territories until the second half of August, when females arrived. Nest-building (8 days) and incubation (16 days) were undertaken entirely by the female, who was not fed on the nest by the male. Chick provisioning was done mainly by the male. Arachnids and terrestrial amphipods were the most common prey brought to chicks. The fledging period was 12 days. Modal clutch size was three eggs, and depredation rates of eggs and chicks were high. After losses, replacement clutches were laid on average 19 days later, after a new nest was built. A maximum of three clutches per pair was recorded. Of 18 eggs monitored, 28% hatched and 17% fledged, equating to a production of one fledgling per pair per year. Ten days after fledging, the entire family leaves the territory, males probably returning once young are independent. The main threats to the local populations are clearing of riparian undergrowth and management practices that impact the predators of rodents.     

Intraspecific nest parasitism in the European starling Sturnus vulgaris

Biochemical genetic markers were used along with conventional methods (abnormal laying sequence/clutch size, unusual egg shape/pigmentation) to identify intraspecific nest parasitism at two British nestbox colonies of the European starling. Between 11 and 37% of first clutches were parasitized during 1977–1979. Parasitic females probably comprised all of the following categories: (1) paired females contesting a nestbox occupied by another pair; (2) previously paired females who had laid a clutch but had been unsuccessful; (3) unpaired females who had copulated with males that already had a mate and nest site; and (4) ‘professional’ nest parasites who distributed at lest some of their eggs in one or more nests other than their own. Although parasitized nests had higher clutch sizes, parasitism led to fewer host young fledging per egg laid, mainly through the eviction of eggs and subsequent nest desertion. Number of parasitic young fledged per egg laid was highest when eggs were laid synchronously with the host, when host clutches were larger, or a smaller number of parasite eggs were added to a nest, thus favouring parasites that distribute their eggs amongst a number of nests. A greater pressure on nest sites may have accounted for the higher levels of parasitism at the Aberdeen colony and for the greater number of parasite eggs laid in a nest. Although most parasitic female starlings appeared to be much less successful than non-parasitic ones, nest parasitism in the starling might evolve directly when one or more of the following advantages are present. (1) There are no constraints on the number of eggs a female may lay but there are constraints on the number of young she may feed adequately. (2) Female survival is increased by having fewer or no eggs/young to care for. (3) Current feeding conditions favour the survival of more young than would be produced by the most common clutch size. Intraspecific nest parasitism is considered to be a first stage in the evolution of interspecific nest parasitism.     

THE EFFECT OF EGG WEIGHT ON THE SUBSEQUENT GROWTH OF NESTLING GREAT TITS PARUS MAJOR

Eggs of known fresh weight were removed from Great Tit nests shortly before hatching and artificially incubated. Four to eight chicks were returned to each nest-box on their hatching day and reared by foster parents. The effect of egg weight on subsequent growth was studied for 81 nestlings (13 broods), 50 of them (8 broods) up to the 17th day.
Hatching success of 275 eggs in the incubator was 67·6% and was not correlated with egg weight.
Egg weight had a significant effect on nestling weight up to the 14th day. Young hatched from lighter eggs grew more slowly at the beginning, but recovered before fledging. Mortality after fledging seemed not to be influenced by egg weight.
Maximum weight (mean 19 g) was attained between the 12th and the 17th day and was positively correlated with egg weight.
The effect of brood-size (small in the experiments) on growth increased significantly with age. The range of egg weight for a nest had a significant effect on growth at the beginning, but a small and not significant effect after the 10th day.
The growth of each brood on any particular day was expressed as a deviation from mean growth. These growth deviations, plotted against date, were similar in all nests and were not correlated with any weather data.
The fledging success of 260 early broods was independent of egg weight, but it was positively correlated with egg weight in 78 late broods (data from 1965–71).
The ecological importance of egg weight at different times of the breeding season is discussed.     

Optimal brood size and its limiting factors in the Rufous Turtle DoveStreptopelia orientalis

Optimal brood size and its limiting factors of the Rufous Turtle Dove,Streptopelia orientalis, were studied at the campus of the University of Tsukuba, Japan, during the breeding season in 1990–92. The dove usually lays two eggs in a nest. I made nests of a brood size of one and three by transferring a hatchling from one nest to the other, and compared their fledging success, factors of breeding failure, weight and tarsus length at fledging, growth rate and nestling period with those of a brood of two. The index of fitness (fledgling weight multiplied by average number of fledglings per nest) was almost the same in broods of two and three. However, the highest variation in fledging weight within the brood and the extension of nestling period were observed in broods of three, which caused the extension of inter-brood interval and consequently the smaller number of broods in the total breeding season. Therefore, broods of three would not have an advantage in producing more offspring than broods of two. Crop milk production had an effect on the growth of nestlings in the early phase of the nestling period, but the rapid growth in the granivorous phase compensated for the growth delay of the smallest nestling in broods of three. Small brood size and a large number of broods in a season would also be more effective under high predation pressure.     

Energy expenditure, nestling age, and brood size: an experimental study of parental behavior in the great tit Parus major

A brood manipulation experiment on great tits Parus major was performedto study the effects of nestling age and brood size on parentalcare and offspring survival. Daily energy expenditure (DEE)of females feeding nestlings of 6 and 12 days of age was measuredusing the doubly-labeled water technique. Females adjusted theirbrooding behavior to the age of the young. The data are consistentwith the idea that brooding behavior was determined primarilyby the thermoregulatory requirements of the brood. Female DEEdid not differ with nestling age; when differences in body masswere controlled for, it was lower during the brooding periodthan later. In enlarged broods, both parents showed significantlyhigher rates of food provisioning to the brood. Female DEE wasaffected by brood size manipulation, and it did not level offwith brood size. There was no significant effect of nestlingage on the relation between DEE and manipulation. Birds wereable to raise a larger brood than the natural brood size, althoughlarger broods suffered from increased nestling mortality ratesduring the peak demand period of the nestlings. Offspring conditionat fledging was negatively affected by brood size manipulation,but recruitment rate per brood was positively related to broodsize, suggesting that the optimal brood size exceeds the naturalbrood size in this population.     

Growth of nestling sparrowhawks (Accipiter nisus)

Growth rates, mortality and parental care of nestling sparrowhawks were studied in southwest Scotland. Ae Forest was a conifer plantation 200–400 metres above sea-level, while the Annan valley consisted of farmland, woods, and small plantations on low ground.
Nestling sparrowhawks were measured daily from hatching for 21–24 days. Weight, tarsus length and outermost primary feather length were recorded. Nestlings could be sexed by the age of 16 days from the larger size of females, which were significantly heavier than males at one day, had longer tarsi at nine days, and longer primaries at 18 days. Growth rates were calculated using linear regression over standardized periods of about 10 days.
Growth rates were independent of brood size, and were negatively correlated with hatching date in one area. Hatching order and growth rate were correlated within broods. The greatest differences in growth rates were found between zones of Ae Forest, and between forest and valley.
Twenty-one per cent of nestlings over two days old died. Causes of mortality were starvation, wet weather, predation and desertion. Most of the mortality occurred in parts of Ae Forest remote from valley woodlands.
The presence or absence of the adult female was noted on nest visits. When habitually brooding, until the young were 11 days old, the hen was present on about 85% of visits. By fledging this figure fell to 66% in the valley, and to 32% in the forest.
The development of sexual dimorphism is discussed; females gained weight and body size faster than males, which developed various skills sooner.
It is suggested that differences in growth rates between parts of the study area were related to food supply. Poor growth rates, high mortality, and lack of parental care all occurred in areas which were remote from sources of abundant prey, as measured by song-bird censuses.     

Maternal behavior and clutch manipulation in the ring-legged earwig (Dermaptera: Carcinophoridae)

The expression and maintenance of maternal behavior in the earwig,Euborellia annulipes, was examined through manipulation of clutch size, age, and species and through observations of interactions between brooding females. Females underwent discrete gonadotrophic cycles culminating in oviposition of first clutches that were highly variable in size. Neither the head capsule width nor the age of the mother was correlated with clutch size. Maternal care extended through embryogenesis and for the week following hatching. Clutch removal significantly shortened the interclutch interval, indicating that the presence of brood inhibited the onset of the second gonadotrophic cycle. Brooding females readily accepted replacement clutches of the same age. Thus, mothers did not appear to distinguish their own eggs from those of other females. Experimental doubling of clutch size did not significantly reduce the proportion hatching or fledging. In contrast, reducing clutch size diminished the percentage successfully fledging. Manipulation of clutch age resulted in reduced hatching/fledging success. Placing two females, each with newly laid clutches, in the same cage usually resulted in egg transfer from the nest of one female to that of the other within 12 h. Nests of females with larger forceps were significantly more likely to contain both clutches. When mothers with first clutches were paired with mothers with third clutches, eggs were more likely to be transferred to the nest of the older female.E. annulipes females with newly laid clutches appeared to accept as replacement clutches eggs of the earwigDoru taeniatum. Alien clutches were maintained for the typical duration of embryogenesis; however, noD. taeniatum hatchlings were observed.     

Experimental analysis of mass change in female green-rumped parrotlets (Forpus passerinus): the role of male cooperation

Mass change was determined by weighing nine unmanipulated pairsof green-rumped parrodets during prospecting, egg laying, hatching,and fledging. Male and female mass were similar at the onsetof prospecting. However, female mass had increased 25% by thestart of egg laying, and females maintained the heavy mass throughincubation. Females began losing mass at the time of hatchingand reverted to weights that were similar to those of malesby the end of hatching. Males neither gained nor lost mass duringbreeding. To test predictions from mass change hypotheses, 25females were assigned manipulated broods of four or eight young.Females were weighed on the first day of hatching and 6, 10,and 27 days later, or until first fledging. Females with fourand eight young lost the same amount of mass. Females lost lessmass during brooding if their mates fed them more often. Femaleswith four young tended to lose less mass during brooding ifthey spent less time away from the nest, whereas females witheight young tended to lose less mass if they spent more timeaway from the nest. Mass change after brooding was not relatedto provisioning rates of nestlings by females or males of eitherexperimental group. Our results contradict the hypothesis thatmass loss is due to stress, and correspond to some of the predictionsof the adaptive, gonadal, and brooding starvation hypotheses.     

Breeding biology of the Barn Owl Tyto alba in central Mali

Data were obtained on 178 clutches of African Barn Owls in central Mali from four breeding seasons during 1979–1983. Significantly more clutches were laid in 1979–1980 and significantly fewer in 1980– 1981 than the average for the 4 years and there were significantly more clutches laid in the middle period of the annual breeding season. The egg volume was significantly smaller at the beginning of the breeding season and significantly larger in the middle than the overall mean with eggs of second clutches being larger than those of first clutches. The clutch size was 605 eggs of which 479 hatched. The number of young fledged per successful nest was 319 and was 1 83 for all nesting attempts. The month was the only variable shown to affect significantly the clutch size, eggs hatched and fledging rate, the highest success rates being associated with the middle of the breeding period. The average interval between the hatching of eggs was 2–31 days. Survival rates (47'1%) to fledging were significantly affected by year (1981–1982 being the least) and month (mid-season birds the best). The order of hatching significantly affected age at death or disappearance, the first-hatched birds surviving the longest. The year significantly affected age at fledging, the young from the year in which most clutches were laid leaving the nest at the youngest age and those associated with the year having the least number of clutches remaining in the nest the longest. The month of hatching also affected fledging age, birds at the extremes of the breeding season fledging at older ages. The discussion compares these data with those from elsewhere.     

Experimentally Constrained Virulence is Costly for Common Cuckoo Chicks

Chicks of some avian brood parasites show high virulence by eliminating all host progeny in the nest whereas others develop in the presence of host nestmates. Common cuckoo ( Cuculus canorus ) chicks are typically highly virulent parasites as they attempt to evict all host eggs and chicks soon after hatching. However, several features of nest design, including steep walls and/or cavity nests, may effectively prevent cuckoo hatchlings from evicting nestmates. A previous observational study showed low success of cuckoo chicks in evicting progeny of a cavity nester host, the redstart ( Phoenicurus phoenicurus ) but cuckoo chicks showed low survival both when reared alone or in mixed broods with host nestmates. Whether poor cuckoo performance was caused by eviction costs and/or by the effect of presence of host chicks per se remains unclear. We experimentally cancelled any potential eviction costs by removing host eggs immediately after the cuckoo hatched and creating mixed broods 5 days later when the eviction instinct of the cuckoo already ceased. Cuckoos that were forced to compete with host nestlings experienced lower provisioning rates, poorer growth, and lower fledging success than control lone cuckoos. Cuckoos in mixed broods that survived until fledging fledged later, and at lower masses, than those in the sole cuckoo group. Thus, the cuckoo gens specializing on redstarts is similar to other cuckoo gentes, whose chicks are more successful in evicting host nestmates, and it does not benefit from the presence of host brood. Cohabitation with host nestlings then should be viewed as a maladaptive by-product of host cavity nest design.     

Parental care behavior in the monogamous,sexually dimorphic Madagascar paradise flycatcher: sex differences and the effect of brood size

I studied the parental care behavior of the Madagascar paradise flycatcher Terpsiphone mutata in northwestern Madagascar. I especially focused on feeding, brooding and vigilance behaviors. Feeding rate did not differ between males and females, but females spent more time at the nest than males. Females dedicated their time to brooding, while males perched on the nest and were vigilant. Both parents changed the feeding rate in relation to brood size, so the feeding rate per nestling was not different among nests of different brood size. Duration of brooding by females increased with decreasing brood size, suggesting that the Royama effect, the pattern of lower feeding rate per nestling in larger broods, did not apply in this study. Males spent more time on vigilance than females. Anti-predator vigilance by males should be important for nestling survival given the high predation pressure typical of this population. In conclusion, males provide considerable parental care probably to minimize nestling starvation and to avoid nest predation. My results are not consistent with the general pattern of less parental effort by males in monogamous, sexually dimorphic species.